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T11479GSK1521498；化合物 T11479GSK1521498
GSK1521498 is a selective antagonist of the μ-opioid receptor (MOR). It is being used for the treatment of disorders of compulsive consumption of food, alcohol, and drugs.
价 格：￥电议型 号：T11479产 地：中国大陆
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T11478LGSK1521498 free base；化合物 T11478LGSK1521498 free base
GSK1521498 free base is a potent and selective antagonist of the μ-opioid receptor. GSK1521498 free base also has the potential for disorders of compulsive consumption of food, alcohol, and drugs.
价 格：￥电议型 号：T11478L产 地：中国大陆
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T11478GSK1521498 free base (hydrochloride)；化合物 T11478GSK1521498 free base (hydrochloride)
GSK1521498 free base (hydrochloride) is a selective antagonist of the μ-opioid receptor (MOR). It is being used for the treatment of disorders of compulsive consumption of food, alcohol, and drugs.
价 格：￥电议型 号：T11478产 地：中国大陆
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T11415Glucagon receptor antagonists-3；化合物 T11415Glucagon receptor antagonists-3
Glucagon receptor antagonist -3 is a highly effective glucagon receptor antagonist.
价 格：￥电议型 号：T11415产 地：中国大陆
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T11395GF 15；化合物 T11395GF 15
GF 15 is a potent inhibitor of centrosomal clustering in tumor cells.
价 格：￥电议型 号：T11395产 地：中国大陆
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T1137Clorsulon；氯舒隆L631529|||MK401；克洛索隆|||L631529|||MK401|||氯舒隆
Clorsulon (L631529) is utilized for the treatment of Fasciola hepatica infections in calves and sheep.
价 格：￥电议型 号：T1137产 地：中国大陆
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T11344G150；化合物G150G150
G150 inhibited interferon expression triggered by DSDNA with IC50 of 10.2 nM.G150 is an effective and highly selective inhibitor of human cyclic GMP-AMP synthase (H-CGAS).
价 格：￥电议型 号：T11344产 地：中国大陆
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T11328FT-1518；化合物 T11328FT-1518
FT-1518 ,exhibits antitumor activity, is a new generation selective, potent and oral bioavailable mTORC1 and mTORC2 inhibitor.
价 格：￥电议型 号：T11328产 地：中国大陆
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T11315Fosmidomycin sodium salt膦胺霉素钠盐FR-31564 sodium salt
Fosmidomycin sodium salt (FR-31564 sodium salt) is an anti-infective antibiotic with anti-malarial activity that inhibits both Gram-negative and Gram-positive bacteria.
价 格：￥电议型 号：T11315产 地：中国大陆
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T11309FMF-04-159-2；化合物 T11309FMF-04-159-2
FMF-04-159-2 inhibits CDK14 and CDK2 with IC50s of 39.6 nM and 256 nM in NanoBRET assay, respectively. FMF-04-159-2 is a covalent CDK14 inhibitor.
价 格：￥电议型 号：T11309产 地：中国大陆
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T11220LUK 227786；化合物T11220Lhydrochloride(150452-18-9 Free base)|||1-[4-(1,3-Benzodioxol-5a-ylmethylamino)-6
UK 227786 is an inhibitor of phosphodiesterase 5 (PDE5), used for treatment of prostatic diseases.
价 格：￥电议型 号：T11220L产 地：中国大陆
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T11215Episilvestrol；化合物 T11215Episilvestrol
Episilvestrol is a specific eIF4A-targeting translation inhibitor, with antitumor activity. Episilvestrol is a derivative of silvestrol, isolated from the fruits and twigs of Aglaia silvestris.
价 格：￥电议型 号：T11215产 地：中国大陆
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T11159EGFR-IN-2；化合物 T11159EGFR-IN-2
EGFR-IN-2 is a non-covalent, mutation-selective and irreversible second-generation EGFR inhibitor.
价 格：￥电议型 号：T11159产 地：中国大陆
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T11158EGFR-IN-11；化合物EGFR-IN-11EGFR-IN-11
EGFR-IN-11 is a selective inhibitor of EGFR-tyrosine kinase and induces cell apoptosis. EGFR-IN-11 inhibits triple mutant EGFRL858R/T790M/C797S with an IC50 of 18 nM and arrests cell cycle at G0/G1.
价 格：￥电议型 号：T11158产 地：中国大陆
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T11157LEGFR-IN-1 hydrochloride；EGFR-IN-1盐酸盐EGFR-IN-1 hydrochloride
EGFR-IN-1 hydrochloride is an irreversible and specific inhibitor of L858R/T790M mutant EGFR with 100-fold selectivity over wild-type EGFR. EGFR-IN-1 hydrochloride exhibits potent antitumor and antiproliferative activity in H1975 cells and the mutant HCC827 cells with IC50s of 4 and 28 nM, respectively.
价 格：￥电议型 号：T11157L产 地：中国大陆
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T11157EGFR-IN-1；化合物 T11157EGFR-IN-1
EGFR-IN-1, an orally active and irreversible selective inhibitor targeting L858R/T790M mutant EGFR, exhibits strong antiproliferative and antitumor activity, particularly against H1975 cells and first line mutant HCC827 cells. This compound potently inhibits Gefitinib-resistant EGFR L858R/T790M mutations with a 100-fold selectivity over the wild-type EGFR.
价 格：￥电议型 号：T11157产 地：中国大陆
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T11156LNazartinib mesylate；化合物 T11156LEGF816 (mesylate)；EGF816 (mesylate)
Nazartinib mesylate is a novel, covalent mutant-selective inhibitor of EGFR (Ki and Kinact: 31 nM and 0.222/min on EGFR(L858R/790M) mutant).
价 格：￥电议型 号：T11156L产 地：中国大陆
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T11156Nazartinib S-enantiomer；化合物 T11156EGF816 (S-enantiomer)；EGF816 (S-enantiomer)
Nazartinib is an EGFR inhibitor. Nazartinib S-enantiomer is the less active S-enantiomer of Nazartinib.
价 格：￥电议型 号：T11156产 地：中国大陆
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T11155Eg5 Inhibitor V, trans-24；化合物Eg5 Inhibitor V, trans-24Eg5 Inhibitor V, trans-24
Eg5 Inhibitor V, trans-24 is a specific and potent Eg5 inhibitor that can be used in cancer research with an IC50 value of 0.65 uM.
价 格：￥电议型 号：T11155产 地：中国大陆
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T11154LEG01377 2HCl；EG01377二盐酸盐EG01377 2HCl(2227996-00-9 Free base)；EG01377 2HCl(2227996-00-9 Free base)
EG01377 2HCl is a potent, bioavailable and selective inhibitor of neuropilin-1 (NRP1) with a Kd value of 1.32 μM and an IC50 value of 609 nM for both EG01377 2HCl against NRP1-a1 and NRP1-b1.EG01377 exhibits anti-angiogenic, antimigratory and antitumor activities.
价 格：￥电议型 号：T11154L产 地：中国大陆
